Journal
MOLECULES
Volume 28, Issue 2, Pages -Publisher
MDPI
DOI: 10.3390/molecules28020511
Keywords
Glochidion puberum; triterpenoid; structural elucidation; apoptosis; endoplasmic reticulum stress
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Two new coumaroyl or feruloyl oleananes, Glochidpurnoids A and B (1 and 2), were isolated from the stems and twigs of Glochidion puberum, along with 17 known triterpenoids (3-19). The structures of these compounds were determined using various spectroscopic techniques, chemical methods, and single crystal X-ray diffraction. Cytotoxicity screening against colorectal cancer cell line HCT-116 revealed that compounds 2, 3, 5, 6, 11, and 17 exhibited significant inhibitory activities (IC50: 0.80-2.99 μM), surpassing the positive control 5-fluorouracil (5-FU). Mechanistic study of compound 2, the most potent compound, demonstrated its ability to induce endoplasmic reticulum (ER) stress-mediated apoptosis and enhance the sensitivity of HCT-116 cells to 5-FU.
Glochidpurnoids A and B (1 and 2), two new coumaroyl or feruloyl oleananes, along with 17 known triterpenoids (3-19) were obtained from the stems and twigs of Glochidion puberum. Their structures were elucidated by extensive spectroscopic data analyses, chemical methods, and single crystal X-ray diffraction. All compounds were screened for cytotoxicity against the colorectal cancer cell line HCT-116, and 2, 3, 5, 6, 11, and 17 showed remarkable inhibitory activities (IC50: 0.80-2.99 mu M), being more active than the positive control 5-fluorouracil (5-FU). The mechanistic study of 2, the most potent compound, showed that it could induce endoplasmic reticulum (ER) stress-mediated apoptosis and improve the sensitivity of HCT-116 cells to 5-FU.
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